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硅膜基液-液微界面阵列上生理基质中β受体阻滞剂普萘洛尔的离子转移伏安法测定。

Ion-transfer voltammetric determination of the beta-blocker propranolol in a physiological matrix at silicon membrane-based liquid|liquid microinterface arrays.

机构信息

Tyndall National Institute, Lee Maltings, University College, Cork, Ireland.

出版信息

Anal Chem. 2009 Mar 15;81(6):2344-9. doi: 10.1021/ac802644g.

Abstract

In this work, the ion-transfer voltammetric detection of the protonated beta-blocker propranolol in artificial saliva is presented. Cyclic voltammetry, differential pulse voltammetry, and differential pulse stripping voltammetry (DPSV) were employed in the detection of the cationic drug based on ion-transfer voltammetry across arrays of microinterfaces between artificial saliva and an organogel phase. It was found that the artificial saliva matrix decreased the available potential window for ion-transfer voltammetry at this liquid|liquid interface but transfer of protonated propranolol was still achieved. The DPSV method employed a preconditioning step as well as a preconcentration step followed by analytical signal generation based on the back-transfer of the drug across the array of microinterfaces. The DPSV peak current response was linear with drug concentration in the artificial saliva matrix over the concentration range of 0.05-1 microM (i(p) = -8.13 (nA microM(-1))(concentration) + 0.07 (nA), R = 0.9929, n = 7), and the calculated detection limit (3s(b)) was 0.02 microM. These results demonstrate that DPSV at arrays of liquid|liquid microinterfaces is a viable analytical approach for pharmaceutical determinations in biomimetic matrixes.

摘要

在这项工作中,提出了在人工唾液中质子化的β受体阻滞剂普萘洛尔的离子转移伏安检测。循环伏安法、差分脉冲伏安法和差分脉冲溶出伏安法(DPSV)被用于基于人工唾液和有机凝胶相之间的微界面之间的离子转移伏安法检测阳离子药物。发现人工唾液基质降低了在该液-液界面处的离子转移伏安法的可用电位窗口,但质子化普萘洛尔的转移仍得以实现。DPSV 方法采用了预处理步骤以及预浓缩步骤,然后基于药物通过微界面阵列的反向转移来生成分析信号。DPSV 峰电流响应与人工唾液基质中的药物浓度呈线性关系,浓度范围为 0.05-1 microM(i(p) = -8.13 (nA microM(-1))(浓度) + 0.07 (nA),R = 0.9929,n = 7),计算出的检测限(3s(b))为 0.02 microM。这些结果表明,在液体-液体微界面的阵列上进行 DPSV 是一种可行的分析方法,可用于仿生基质中的药物测定。

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